Canonical Allele Identifier: CA376840612

Gene: MYPN

Linked Data

• ClinVar Variation Id: 1781883
• ClinVar RCV Id: RCV002415300
• MyVariant Identifiers: chr10:g.69926330C>A (hg19) ; chr10:g.68166573C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166573C>A , CM000672.2:g.68166573C>A	GRCh38
NC_000010.10:g.69926330C>A , CM000672.1:g.69926330C>A	GRCh37
NC_000010.9:g.69596336C>A	NCBI36
NG_032118.1:g.65457C>A , LRG_410:g.65457C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1055C>A	ENSP00000346369.2:p.Ser352Tyr
ENST00000373675.4:c.1880C>A	ENSP00000362779.4:p.Ser627Tyr
ENST00000540630.6:c.1934C>A	ENSP00000441668.3:p.Ser645Tyr
ENST00000613327.5:c.1880C>A	ENSP00000480757.2:p.Ser627Tyr
ENST00000687572.1:c.758C>A	ENSP00000510427.1:p.Ser253Tyr
ENST00000688812.1:c.1856C>A	ENSP00000510658.1:p.Ser619Tyr
ENST00000690544.1:c.*1151C>A	ENSP00000508989.1:n.*1151C>A
ENST00000358913.10:c.1880C>A MANE Select	ENSP00000351790.5:p.Ser627Tyr
ENST00000354393.6:c.1055C>A	ENSP00000346369.2:p.Ser352Tyr
ENST00000358913.9:c.1880C>A	ENSP00000351790.5:p.Ser627Tyr
ENST00000540630.5:c.1880C>A	ENSP00000441668.2:p.Ser627Tyr
ENST00000613327.4:c.998C>A	ENSP00000480757.1:p.Ser333Tyr
NM_001256267.1:c.1880C>A	NP_001243196.1:p.Ser627Tyr
NM_001256268.1:c.998C>A	NP_001243197.1:p.Ser333Tyr
NM_032578.3:c.1880C>A , LRG_410t1:c.1880C>A	NP_115967.2:p.Ser627Tyr
NR_045662.3:n.1307C>A
NR_045663.3:n.2148C>A
XM_006718043.2:c.1934C>A	XP_006718106.1:p.Ser645Tyr
XM_011540292.1:c.1910C>A	XP_011538594.1:p.Ser637Tyr
XM_017016833.1:c.1958C>A	XP_016872322.1:p.Ser653Tyr
XM_017016834.2:c.1880C>A	XP_016872323.1:p.Ser627Tyr
XM_024448236.1:c.758C>A	XP_024304004.1:p.Ser253Tyr
NR_045662.4:n.1417C>A
NR_045663.4:n.2093C>A
NM_001256267.2:c.1880C>A	NP_001243196.1:p.Ser627Tyr
NM_001256268.2:c.998C>A	NP_001243197.1:p.Ser333Tyr
NM_032578.4:c.1880C>A MANE Select	NP_115967.2:p.Ser627Tyr